Canonical Allele Identifier: CA2557048273

Gene: MAGI2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.78413854_78413855insCAG , CM000669.2:g.78413854_78413855insCAG	GRCh38
NC_000007.13:g.78043171_78043172insCAG , CM000669.1:g.78043171_78043172insCAG	GRCh37
NC_000007.12:g.77881107_77881108insCAG	NCBI36
NG_011487.1:g.1044719_1044720insCTG
NG_011487.2:g.1044720_1044721insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354212.9:c.1046-44642_1046-44641insCTG MANE Select	ENSP00000346151.4:n.1046-44642_1046-44641insCTG
ENST00000636039.1:c.116-44642_116-44641insCTG	ENSP00000490259.1:n.116-44642_116-44641insCTG
ENST00000636178.1:c.116-44642_116-44641insCTG	ENSP00000489709.1:n.116-44642_116-44641insCTG
ENST00000636717.1:c.542-44642_542-44641insCTG	ENSP00000490128.1:n.542-44642_542-44641insCTG
ENST00000637074.1:n.32-44642_32-44641insCTG
ENST00000637282.1:c.-128-44642_-128-44641insCTG	ENSP00000490637.1:n.-128-44642_-128-44641insCTG
ENST00000637441.1:c.1046-44642_1046-44641insCTG	ENSP00000489633.1:n.1046-44642_1046-44641insCTG
ENST00000637486.1:c.557-44642_557-44641insCTG	ENSP00000490080.1:n.557-44642_557-44641insCTG
ENST00000354212.8:c.1046-44642_1046-44641insCTG	ENSP00000346151.4:n.1046-44642_1046-44641insCTG
ENST00000419488.5:c.1046-44642_1046-44641insCTG	ENSP00000405766.1:n.1046-44642_1046-44641insCTG
ENST00000519748.5:c.-128-44642_-128-44641insCTG	ENSP00000486774.1:n.-128-44642_-128-44641insCTG
ENST00000520379.2:n.121-44642_121-44641insCTG
ENST00000522391.3:c.1046-44642_1046-44641insCTG	ENSP00000428389.1:n.1046-44642_1046-44641insCTG
ENST00000535697.5:c.632-44642_632-44641insCTG	ENSP00000441603.3:n.632-44642_632-44641insCTG
ENST00000626691.2:c.557-44642_557-44641insCTG	ENSP00000486131.1:n.557-44642_557-44641insCTG
ENST00000628781.1:c.557-44642_557-44641insCTG	ENSP00000485970.1:n.557-44642_557-44641insCTG
ENST00000628980.2:c.632-44642_632-44641insCTG	ENSP00000487526.1:n.632-44642_632-44641insCTG
ENST00000629359.2:c.557-44642_557-44641insCTG	ENSP00000487448.1:n.557-44642_557-44641insCTG
ENST00000630991.2:c.377-44642_377-44641insCTG	ENSP00000487435.1:n.377-44642_377-44641insCTG
ENST00000634996.1:c.-128-44642_-128-44641insCTG	ENSP00000489533.1:n.-128-44642_-128-44641insCTG
NM_001301128.1:c.1046-44642_1046-44641insCTG	NP_001288057.1:n.1046-44642_1046-44641insCTG
NM_012301.3:c.1046-44642_1046-44641insCTG	NP_036433.2:n.1046-44642_1046-44641insCTG
XM_011516718.1:c.1046-44642_1046-44641insCTG	XP_011515020.1:n.1046-44642_1046-44641insCTG
XM_011516719.1:c.557-44642_557-44641insCTG	XP_011515021.1:n.557-44642_557-44641insCTG
XM_011516720.1:c.557-44642_557-44641insCTG	XP_011515022.1:n.557-44642_557-44641insCTG
XM_011516721.1:c.557-44642_557-44641insCTG	XP_011515023.1:n.557-44642_557-44641insCTG
XM_011516722.1:c.377-44642_377-44641insCTG	XP_011515024.1:n.377-44642_377-44641insCTG
XM_011516723.1:c.1046-44642_1046-44641insCTG	XP_011515025.1:n.1046-44642_1046-44641insCTG
XM_011516724.1:c.1046-44642_1046-44641insCTG	XP_011515026.1:n.1046-44642_1046-44641insCTG
XM_011516725.1:c.1046-44642_1046-44641insCTG	XP_011515027.1:n.1046-44642_1046-44641insCTG
XM_011516726.1:c.-128-44642_-128-44641insCTG	XP_011515028.1:n.-128-44642_-128-44641insCTG
XM_011516727.1:c.-129+35087_-129+35088insCTG	XP_011515029.1:n.-129+35087_-129+35088insCTG
XM_011516728.1:c.-128-44642_-128-44641insCTG	XP_011515030.1:n.-128-44642_-128-44641insCTG
XM_011516729.1:c.-128-44642_-128-44641insCTG	XP_011515031.1:n.-128-44642_-128-44641insCTG
XM_011516718.2:c.1046-44642_1046-44641insCTG	XP_011515020.1:n.1046-44642_1046-44641insCTG
XM_011516719.3:c.557-44642_557-44641insCTG	XP_011515021.1:n.557-44642_557-44641insCTG
XM_011516720.3:c.557-44642_557-44641insCTG	XP_011515022.1:n.557-44642_557-44641insCTG
XM_011516726.3:c.-128-44642_-128-44641insCTG	XP_011515028.1:n.-128-44642_-128-44641insCTG
XM_017012840.2:c.1046-44642_1046-44641insCTG	XP_016868329.1:n.1046-44642_1046-44641insCTG
XM_017012841.2:c.1046-44642_1046-44641insCTG	XP_016868330.1:n.1046-44642_1046-44641insCTG
XM_017012842.2:c.1046-44642_1046-44641insCTG	XP_016868331.1:n.1046-44642_1046-44641insCTG
XM_017012843.2:c.1046-44642_1046-44641insCTG	XP_016868332.1:n.1046-44642_1046-44641insCTG
XM_017012844.2:c.1046-44642_1046-44641insCTG	XP_016868333.1:n.1046-44642_1046-44641insCTG
XM_017012845.2:c.1046-44642_1046-44641insCTG	XP_016868334.1:n.1046-44642_1046-44641insCTG
XM_017012846.2:c.1046-44642_1046-44641insCTG	XP_016868335.1:n.1046-44642_1046-44641insCTG
XM_017012847.2:c.557-44642_557-44641insCTG	XP_016868336.1:n.557-44642_557-44641insCTG
XM_017012848.2:c.557-44642_557-44641insCTG	XP_016868337.1:n.557-44642_557-44641insCTG
XM_017012849.2:c.557-44642_557-44641insCTG	XP_016868338.1:n.557-44642_557-44641insCTG
XM_017012850.2:c.1046-44642_1046-44641insCTG	XP_016868339.1:n.1046-44642_1046-44641insCTG
XM_017012851.2:c.1046-44642_1046-44641insCTG	XP_016868340.1:n.1046-44642_1046-44641insCTG
XM_017012852.2:c.1046-44642_1046-44641insCTG	XP_016868341.1:n.1046-44642_1046-44641insCTG
XM_024447009.1:c.557-44642_557-44641insCTG	XP_024302777.1:n.557-44642_557-44641insCTG
NM_012301.4:c.1046-44642_1046-44641insCTG MANE Select	NP_036433.2:n.1046-44642_1046-44641insCTG
NM_001301128.2:c.1046-44642_1046-44641insCTG	NP_001288057.1:n.1046-44642_1046-44641insCTG